Efficacy of Keyhole Approach to Carpal Tunnel Syndrome under Ambulatory Strategy

Por Ramos-Zúñiga, Rodrigo, García-Mercado, César J., Segura-Durán, Iván, Zepeda-Gutiérrez, Luis A.
Publicado no Neurol Res Int (2017)

Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

Por Marques, Felipe, Tenney, Jessica, Duran, Ivan, Martin, Jorge, Nevarez, Lisette, Pogue, Robert, Krakow, Deborah, Cohn, Daniel H., Li, Bing
Publicado no PLoS Genet (2016)

Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

Por Marques, Felipe, Tenney, Jessica, Duran, Ivan, Martin, Jorge, Nevarez, Lisette, Pogue, Robert, Krakow, Deborah, Cohn, Daniel H., Li, Bing
Publicado no PLoS Genet (2016)

HSP47 and FKBP65 cooperate in the synthesis of type I procollagen

Por Duran, Ivan, Nevarez, Lisette, Sarukhanov, Anna, Wu, Sulin, Lee, Katrina, Krejci, Pavel, Weis, Maryann, Eyre, David, Krakow, Deborah, Cohn, Daniel H.
Publicado no Hum Mol Genet (2015)

Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome

Por Taylor, S. Paige, Dantas, Tiago J., Duran, Ivan, Wu, Sulin, Lachman, Ralph S., Nelson, Stanley F., Cohn, Daniel H., Vallee, Richard B., Krakow, Deborah
Publicado no Nat Commun (2015)

Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome

Por Duran, Ivan, Taylor, S. Paige, Zhang, Wenjuan, Martin, Jorge, Forlenza, Kimberly N., Spiro, Rhonda P., Nickerson, Deborah A., Bamshad, Michael, Cohn, Daniel H., Krakow, Deborah
Publicado no Sci Rep (2016)

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

Por Zieba, Jennifer, Forlenza, Kimberly Nicole, Khatra, Jagteshwar Singh, Sarukhanov, Anna, Duran, Ivan, Rigueur, Diana, Lyons, Karen M., Cohn, Daniel H., Merrill, Amy E., Krakow, Deborah
Publicado no PLoS Genet (2016)

Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia

Por Duran, Ivan, Taylor, S. Paige, Zhang, Wenjuan, Martin, Jorge, Qureshi, Faisal, Jacques, Suzanne M., Wallerstein, Robert, Lachman, Ralph S., Nickerson, Deborah A., Bamshad, Michael, Cohn, Daniel H., Krakow, Deborah
Publicado no Cilia (2017)

An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndrome

Por Paige Taylor, S., Kunova Bosakova, Michaela, Varecha, Miroslav, Balek, Lukas, Barta, Tomas, Trantirek, Lukas, Jelinkova, Iva, Duran, Ivan, Vesela, Iva, Forlenza, Kimberly N., Martin, Jorge H., Hampl, Ales, Bamshad, Michael, Nickerson, Deborah, Jaworski, Margie L., Song, Jieun, Ko, Hyuk Wan, Cohn, Daniel H., Krakow, Deborah, Krejci, Pavel
Publicado no Hum Mol Genet (2016)

The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery

Por Toriyama, Michinori, Lee, Chanjae, Taylor, S. Paige, Duran, Ivan, Cohn, Daniel H., Bruel, Ange-Line, Tabler, Jacqueline M., Drew, Kevin, Kelley, Marcus R., Kim, Sukyoung, Park, Tae Joo, Braun, Daniella, Pierquin, Ghislaine, Biver, Armand, Wagner, Kerstin, Malfroot, Anne, Panigrahi, Inusha, Franco, Brunella, Al-lami, Hadeel Adel, Yeung, Yvonne, Choi, Yeon Ja, Duffourd, Yannis, Faivre, Laurence, Rivière, Jean-Baptiste, Chen, Jiang, Liu, Karen J., Marcotte, Edward M., Hildebrandt, Friedhelm, Thauvin-Robinet, Christel, Krakow, Deborah, Jackson, Peter K., Wallingford, John B.
Publicado no Nat Genet (2016)